Modeling an Optimal 3D Skin-on-Chip within Microfluidic Devices for Pharmacological Studies.
ECM
TEER
cosmetic test
dermatology
immune system
microbiome
microfluidic devices
pharmacological test
skin-on-chip
toxicological test
Journal
Pharmaceutics
ISSN: 1999-4923
Titre abrégé: Pharmaceutics
Pays: Switzerland
ID NLM: 101534003
Informations de publication
Date de publication:
06 Jul 2022
06 Jul 2022
Historique:
received:
07
06
2022
revised:
27
06
2022
accepted:
05
07
2022
entrez:
27
7
2022
pubmed:
28
7
2022
medline:
28
7
2022
Statut:
epublish
Résumé
Preclinical research remains hampered by an inadequate representation of human tissue environments which results in inaccurate predictions of a drug candidate's effects and target's suitability. While human 2D and 3D cell cultures and organoids have been extensively improved to mimic the precise structure and function of human tissues, major challenges persist since only few of these models adequately represent the complexity of human tissues. The development of skin-on-chip technology has allowed the transition from static 3D cultures to dynamic 3D cultures resembling human physiology. The integration of vasculature, immune system, or the resident microbiome in the next generation of SoC, with continuous detection of changes in metabolism, would potentially overcome the current limitations, providing reliable and robust results and mimicking the complex human skin. This review aims to provide an overview of the biological skin constituents and mechanical requirements that should be incorporated in a human skin-on-chip, permitting pharmacological, toxicological, and cosmetic tests closer to reality.
Identifiants
pubmed: 35890312
pii: pharmaceutics14071417
doi: 10.3390/pharmaceutics14071417
pmc: PMC9316928
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
Subventions
Organisme : Gobierno de Aragón
ID : GIS096
Organisme : Gobierno de Aragón
ID : LMP233_21
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